Synopsis
Synopsis
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USDMF
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EU WC
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KDMF
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NDC API
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VMF
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EDQM
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USP
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JP
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FDF Dossiers
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FDA Orange Book
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Europe
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Canada
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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US Medicaid
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Data Compilation #PharmaFlow
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1. 2 Alpha,17 Alpha-dimethyldihydrotestosterone
2. 2,17-dimethyldihydrotestosterone
1. Superdrol
2. 3381-88-2
3. Methasteron
4. Methyldrostanolone
5. (2r,5s,8r,9s,10s,13s,14s,17s)-17-hydroxy-2,10,13,17-tetramethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1h-cyclopenta[a]phenanthren-3-one
6. Gh88dy98mr
7. 2alpha,17alpha-dimethyldihydrotestosterone
8. Nsc-40490
9. 17beta-hydroxy-2alpha,17-dimethyl-5alpha-androstan-3-one
10. 17a-methyl-drostanolone
11. 17-methyldrostanolone
12. 2,17-dimethyldihydrotestosterone
13. Nsc 40490
14. Unii-gh88dy98mr
15. Methasterone [who-dd]
16. Schembl4115285
17. Niosh/bv8047800
18. Chebi:79618
19. Dtxsid10187472
20. Nsc40490
21. Zinc4792120
22. Akos015902002
23. Bv80478000
24. Q15409388
25. 2-alpha,17-alpha-dimethyl-17-beta-hydroxy-5-alpha-androstan-3-one
26. 2.alpha.17.alpha.-dimethyletiocholan-3-on-17.beta.-ol
27. 5-alpha-androstan-3-one, 2-alpha,17-alpha-dimethyl-17-beta-hydroxy-
28. 17.beta.-hydroxy-2.alpha.,17.alpha.-dimethyl-5.alpha.-androstane-3-one
29. 2.alpha.,17.alpha.-dimethyl-17.beta.-hydroxy-5.alpha.-androstane-3-one
30. Androstan-3-one, 17-hydroxy-2,17-dimethyl-, (2.alpha.,5.alpha.,17.beta.)-
Molecular Weight | 318.5 g/mol |
---|---|
Molecular Formula | C21H34O2 |
XLogP3 | 4.5 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 0 |
Exact Mass | 318.255880323 g/mol |
Monoisotopic Mass | 318.255880323 g/mol |
Topological Polar Surface Area | 37.3 Ų |
Heavy Atom Count | 23 |
Formal Charge | 0 |
Complexity | 528 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 8 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 1 |
ABOUT THIS PAGE
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PharmaCompass offers a list of Methasterone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Methasterone manufacturer or Methasterone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methasterone manufacturer or Methasterone supplier.
PharmaCompass also assists you with knowing the Methasterone API Price utilized in the formulation of products. Methasterone API Price is not always fixed or binding as the Methasterone Price is obtained through a variety of data sources. The Methasterone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Methyldrostanolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methyldrostanolone, including repackagers and relabelers. The FDA regulates Methyldrostanolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methyldrostanolone API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Methyldrostanolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methyldrostanolone supplier is an individual or a company that provides Methyldrostanolone active pharmaceutical ingredient (API) or Methyldrostanolone finished formulations upon request. The Methyldrostanolone suppliers may include Methyldrostanolone API manufacturers, exporters, distributors and traders.
click here to find a list of Methyldrostanolone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Methyldrostanolone Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Methyldrostanolone GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Methyldrostanolone GMP manufacturer or Methyldrostanolone GMP API supplier for your needs.
A Methyldrostanolone CoA (Certificate of Analysis) is a formal document that attests to Methyldrostanolone's compliance with Methyldrostanolone specifications and serves as a tool for batch-level quality control.
Methyldrostanolone CoA mostly includes findings from lab analyses of a specific batch. For each Methyldrostanolone CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Methyldrostanolone may be tested according to a variety of international standards, such as European Pharmacopoeia (Methyldrostanolone EP), Methyldrostanolone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Methyldrostanolone USP).